Boris Rolinski - Concepedia

Author

Boris Rolinski

Ludwig-Maximilians-Universität München

Also Known As

B Rolinski, B. Rolinski, Boris Rolinski, Rolinski, B.

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Helmholtz Zentrum München Technical University of Munich München Klinik Paracelsus Medical University

About

Boris Rolinski is an author at Ludwig-Maximilians-Universität München specializing in medicine, metabolism, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	1.4K
2	Health Sciences	2	2	51
3	Education	1	1	42
4	Natural Sciences	1	1	13
5	Public Health	1	1	51

Boris Rolinski

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Megalin Knockout Mice as an Animal Model of Low Molecular Weight Proteinuria Jörg-Robert Leheste, Boris Rolinski, Henrik Vorum, American Journal Of Pathology Knockout MouseGlomerulonephritisUrologyRenal FunctionMedicine	1999	438
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency Tobias B. Haack, Katharina Danhauser, Birgit Haberberger, Nature Genetics Mendelian DisorderIdentifies Acad9 MutationsGenetic DisorderGeneticsMolecular Biology	2010	248
Mitochondrial and Cytosolic Branched-chain Amino Acid Transaminases from Yeast, Homologs of the myc Oncogene-regulated Eca39 Protein Gyula Kispál, Harald Steiner, Deborah A. Court, Journal of Biological Chemistry	1996	171
Bilirubin Measurement for Neonates: Comparison of 9 Frequently Used Methods Karina Grohmann, Markus Roser, Boris Rolinski, PEDIATRICS	2006	127
Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway Johannes A. Mayr, Peter Freisinger, Kurt Schlachter, The American Journal of Human Genetics Thiamine Pyrophosphokinase DeficiencyPyruvate Oxidation PathwayBiochemistryPhysiologyInherited Metabolic Disease	2011	120
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy John F. O’Toole, Yangjian Liu, Erica E. Davis, Journal of Clinical Investigation GeneticsRenal PathologyPathologyMitochondrial Localization SignalMolecular Genetics	2010	118
Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency Uwe Ahting, Johannes A. Mayr, Arnaud Vanlander, Frontiers in Genetics Metabolic DisorderIron MetabolismGeneticsGenetic EpidemiologyPathology	2015	95
Homozygous missense mutation in <i>BOLA3</i> causes multiple mitochondrial dysfunctions syndrome in two siblings Tobias B. Haack, Boris Rolinski, Birgit Haberberger, Journal of Inherited Metabolic Disease	2012	93
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including <i>NDUFB9</i> Tobias B. Haack, Florence Madignier, Martina Herzer, Journal of Medical Genetics	2011	91
Liposomal doxorubicin in the treatment of advanced AIDS-related Kaposi-sarcoma Johannes R. Bogner, Ursula Kronawitter, Boris Rolinski, PubMed	1994	84

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